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Liver MetastasesPhase 2NCT02352259

Treatment of Liver Metastases With Electrochemotherapy (ECTJ) Phase II

A Phase 2 study testing Electrochemotherapy, Cliniporator Vitae® and Bleomycin PHC 15 e. (United States Pharmacopeia - USP) in people with Liver Metastases, run by Institute of Oncology Ljubljana at 4 sites in Slovenia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study is prospective, phase II study, The primary objective of the study is evaluation of the feasibility and safety of intraoperative electrochemotherapy of colorectal liver metastases. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Liver Metastases
What is being tested?
Electrochemotherapy, Cliniporator Vitae® and Bleomycin PHC 15 e. (United States Pharmacopeia - USP)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
23 participants
Where
4 sitesSlovenia
Study dates
Sep 2013to Oct 2018
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Histologically and/or cytologically confirmed colorectal cancer.
  • Age over 18.
  • Life expectancy more than 3 month.
  • Performance status Karnofsky ≥ 70 or (World Health Organization) WHO ≤ 2.
  • Chemotherapy free interval 2-5 weeks, depending on the drugs used.
  • Patient must be mentally capable of understanding the information given.
  • Patient must give informed consent.
  • Patient must be discussed at the multidisciplinary team for tumors of the gastrointestinal tract before entering the trial.

Who cannot join

  • Secondary primary tumor, except surgically treated noninvasive cancer of cervix, or surgically or irradiated basal cell carcinoma
  • Visceral, bone or diffuse metastases.
  • Life-threatening infection and/or heart failure and/or liver failure and/or other severe systemic pathologies.
  • Clinically significant ascites.
  • Significant reduction in respiratory function.
  • Age less than 18 years.
Show all 15Show fewer
  • Coagulation disturbances.
  • Cumulative dose of 250 mg/m2 bleomycin received.
  • Allergic reaction to bleomycin.
  • Impaired kidney function (creatinin > 150 µmol/l).
  • Patients with epilepsy.
  • Patients with arrhythmias.
  • Patients with pacemaker or defibrillator.
  • Pregnancy.
  • Patient incapable of understanding the aim of the study or disagree with the entering into the clinical study.

Trial locations and contacts

4 sites in 1 country.

Slovenia4 sites
  • Faculty of Electrical Engineering, University of Ljubljana, Slovenia

    Ljubljana, 1000

  • Institute of Oncology Ljubljana

    Ljubljana, 1000

  • University Medical Centre Ljubljana, Ljubljana, Slovenia

    Ljubljana, 1000

  • University Medical Centre Maribor, Maribor, Slovenia

    Maribor, 2000

Other trials in Slovenia

About this study

The study is prospective, phase II study, The primary objective of the study is evaluation of the feasibility and safety of intraoperative electrochemotherapy of colorectal liver metastases. The secondary objective is to determine the efficacy of electrochemotherapy treatment, based on histological and radiological evaluation of treated metastases. The endpoints are: toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) ver. 4.0 and response rate measured by percentage of vital tumor cells and mRECIST criteria.

Read the detailed description

The study is an extension of previously concluded and published study on electrochemotherapy of colorectal liver metastases (Edhemovic et al. JSO 2014). In this extension 15 patients will be included. Four groups of patients will be included. The patients from groups 1 and 2 are patients with up to 3 unresectable liver metastases, demanding too excessive resection, or untreatable by standard thermal ablative methods due to the close proximity of major blood vessels. Electrochemotherapy will be offered to these patients as the only treatment option. In case of multiple, both resectable and non-resectable liver metastases, the latter will be treated with electrochemotherapy, whereas other metastases will be resected or treated by RFA. These groups of patients are:

  1. Patients with one to three (1-3) metachronous liver metastases of colorectal cancer, not larger than 5 cm, that are positioned in unresectable liver area, near blood vessels, but in otherwise operable patients.
  2. Recurrent liver metastases of colorectal cancer, not more than 3 and not larger than 5 cm in diameter, each. For those patients any other treatment could represent unacceptable risk due to possibility of insufficient liver residual after resection or less effective radiofrequency ablation due to the proximity of blood vessels. Groups 3 and 4 include patients with intent to cure within standard of care using two-stage surgical approach. This two-stage surgical approach will allow adding electrochemotherapy during the first operation and tissue collection for histological analysis during the second operation. Adding electrochemotherapy to these patients will not affect their treatment within standard of care recommended in the current guidelines. These groups of patients are:
  3. Patients with synchronous metastases, but their general condition and extent of the disease will not allow simultaneous removal of the primary tumor and metastases. During the first operation, the primary tumor will be removed (colorectal resection) and some of the liver metastases will be treated by electrochemotherapy. About 6 weeks later, during the second operation for liver metastases, both treated and non-treated metastases will be removed with liver resection.
  4. Patients with bilateral, multiple, metachronous metastases in whom standard treatment includ two-stage liver resection, due to the extent of the disease and/or their general condition. During the first operation, right portal vein will be ligated and metastases on the left side will be excised or ablated with radiofrequency ablation. At the same time, up to three metastases on the right side were treated with electrochemotherapy. During the second operation, both treated and non-treated metastases on the right side will be removed with right hemihepatectomy.

Electrochemotherapy will be offered to the patients also when they refuse standard treatment.

Depending on the position of metastases, appropriate electrodes will be selected; hexagonal needle electrodes with fixed geometry for metastases not larger than 3 cm in diameter, where their lower edge is located up to 3 cm below the liver capsule. ECT will be performed based on standard operating procedures for treatment of cutaneous and subcutaneous tumors / metastases with ECT.

Individual electrodes, positioned according to the prepared treatment plan will be used for metastases up to 5 cm in diameter, or located near vena cava or large hepatic or portal veins.

Electrochemotherapy will be performed within 8-28 min after intravenous in bolus administration of bleomycin (15 mg/m2).

Triggering of electric pulses will be synchronized with ECG signals, through the ECG triggering device AccuSync to avoid delivery of pulses in vulnerable period of the heart.

All patients will be treated after the procedure has been thoroughly described to them, and have signed informed consent.

Being tested
Electrochemotherapy, Cliniporator Vitae®, Bleomycin PHC 15 e. (United States Pharmacopeia - USP)
Keywords
Liver metastases of colorectal cancer Electrochemotherapy, Bleomycin, Electrochemotherapy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ElectrochemotherapyProcedure or surgery

    Treatment procedure: anesthesia, positioning of electrodes, intravenous in bolus administration of bleomycin, within 8-30 min after administration of bleomycin application of electric pulses, removal of electrodes.

  • Cliniporator Vitae®Device

    Positioning of electrodes, within 8-30 min after administration of bleomycin application of electric pulses (8 pulses, duration 100 microseconds, frequency 4 Hz with amplitude adequate to cover the whole treated lesion with electric field necessary for reversible plasma membrane permeabilization), removal of electrodes.

  • Bleomycin PHC 15 e. (United States Pharmacopeia - USP)Drug

    Intravenous in bolus administration of bleomycin (15 mg/m2), 8 minutes before application of electric pulses

Study groups in NCT02352259
Study groupRoleWhat they receive
ElectrochemotherapyExperimentalNot described
Receives: Procedure: Electrochemotherapy; Device: Cliniporator Vitae®; Drug: Bleomycin PHC 15 e. (United States Pharmacopeia - USP)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Evaluation of Safety Related to Electrochemotherapy

    Recording of adverse events according to CTCAE criteria

    Measured: After operation on day 7

Secondary outcomes (1)
  1. Response to Treatment (Determined by Modified RECIST Criteria).

    Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI/CT:

    Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR

    Measured: After operation on the days 30, 60, 90 and 120

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Feb 2015 (estimated)
  2. Study startSep 2013
  3. Primary completionOct 2018
  4. Study completionOct 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
23 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02352259
Sponsor's protocol ID
03-Z/KESOPKR-28
Status last verified
Mar 2021
First submitted
17 Dec 2014
Last updated
24 Mar 2021
Data monitoring committee
Yes

Publications

  • Edhemovic I, Brecelj E, Gasljevic G, Marolt Music M, Gorjup V, Mali B, Jarm T, Kos B, Pavliha D, Grcar Kuzmanov B, Cemazar M, Snoj M, Miklavcic D, Gadzijev EM, Sersa G. Intraoperative electrochemotherapy of colorectal liver metastases. J Surg Oncol. 2014 Sep;110(3):320-7. doi: 10.1002/jso.23625. Epub 2014 Apr 30.

    PubMed 24782355
  • Edhemovic I, Gadzijev EM, Brecelj E, Miklavcic D, Kos B, Zupanic A, Mali B, Jarm T, Pavliha D, Marcan M, Gasljevic G, Gorjup V, Music M, Vavpotic TP, Cemazar M, Snoj M, Sersa G. Electrochemotherapy: a new technological approach in treatment of metastases in the liver. Technol Cancer Res Treat. 2011 Oct;10(5):475-85. doi: 10.7785/tcrt.2012.500224.

    PubMed 21895032

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Electrochemotherapy, Cliniporator Vitae® and Bleomycin PHC 15 e. (United States Pharmacopeia - USP) in people with Liver Metastases, run by Institute of Oncology Ljubljana at 4 sites in Slovenia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 15 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Mar 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 4 sites in Slovenia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 24 Mar 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Evaluation of Safety Related to Electrochemotherapy (time frame: After operation on day 7). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02352259, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Mar 2021.

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